4.2 Article

Strong linkage disequilibrium at the nucleotide analogue transporter ABCC5 gene locus

Journal

PHARMACOGENETICS AND GENOMICS
Volume 15, Issue 2, Pages 91-104

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01213011-200502000-00005

Keywords

ABCC5; haplotype; linkage disequilibrium; single nucleotide polymorphism; tagging SNP

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The ABCC5 transporter is a ubiquitously expressed ATP-dependent efflux pump that exports nucleotide analogues, including thiopurine anticancer drugs and antiviral drugs. Polymorphisms within this gene may be associated with differences in response to these drugs between different individuals. Haplotype mapping may facilitate the identification of causal genetic variations in association studies. Here, we report the characterization of the haplotype and linkage disequilibrium (LD) profiles across the entire 100 kb of the ABCC5 gene in five ethnically unique populations. Of 24 single nucleotide polymorphisms (SNPs) examined, 16 were observed to occur at high frequency in all five populations and were used for further haplotype and LD analyses. The ABCC5 gene was found to be in strong LD in all populations with half-length LD (LD0.5) estimated to be between 106 and 293 kb long and useful LD extending beyond 100 kb. Low haplotype diversity was observed in the four non-African populations, where the total number of observed haplotypes constituted less than 22% of the predicted number of haplotypes in a simulated population that has undergone maximum recombination. Four and six tagging SNPs, which could account for approximately 90% of observed haplotypes, were identified in the non-African and African-American populations, respectively. (c) 2005 Lippincott Williams & Wilkins.

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